English syllables. 2014.

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  • Iodosobenzene — Chembox new ImageFile =Iodosobenzene.png ImageSize = 120px IUPACName = Iodosobenzene OtherNames = Section1 = Chembox Identifiers CASNo = 536 80 1 PubChem = SMILES = Section2 = Chembox Properties Formula = C6H5IO MolarMass = 220.01 g mol 1… …   Wikipedia

  • iodosobenzene — ˌīəˈdō(ˌ)sō+ noun Etymology: International Scientific Vocabulary iodoso + benzene : an amorphous solid compound C6H5IO that explodes when heated and is formed by treating iodobenzene with chlorine and then with a caustic alkali …   Useful english dictionary

  • Iodobenzene dichloride — Iodobenzene dichloride[1] …   Wikipedia

  • Periodinane — PIFA redirects here. For PIFA (Planar Inverted F Antenna), see Microstrip antenna. The Dess Martin Periodinane Periodinanes are chemical compounds containing hypervalent iodine. These iodine compounds are hypervalent because the iodine atom in it …   Wikipedia

  • Nitrene — The generic structure of a nitrene group In chemistry, a nitrene (R N:) is the nitrogen analogue of a carbene. The nitrogen atom has only 6 valence electrons and is therefore considered an electrophile. A nitrene is a reactive intermediate and is …   Wikipedia

  • Aziridine — Chembox new ImageFileL1 = Aziridine.png ImageSizeL1 = 100px ImageFileR1 = Aziridine3d.png ImageSzieR1 = 100px IUPACName = Aziridine OtherNames = Azacyclopropane, Ethylene imine Section1 = Chembox Identifiers CASNo = 151 56 4 PubChem = SMILES =… …   Wikipedia

  • Viktor Meyer — Infobox Scientist name = Viktor Meyer image width = 200px caption = Viktor Meyer birth date = September 8 1848 birth place = Berlin, Germany residence = Germany, Switzerland nationality = German death date = death date and age|1897|8|8|1848|8|9… …   Wikipedia

  • Ring expansion reaction — A ring expansion reaction is a type of organic reaction in which usually a hydrocarbon ring is expanded. Examples of ring expansions are: * Beckmann rearrangement * Dowd Beckwith ring expansion reaction. Ring contraction reaction A ring… …   Wikipedia

  • Stetter reaction — The Stetter reaction is an organic reaction involving the nucleophile catalyzed conjugate addition of an aldehyde to a Michael acceptor such as an enone Ref|Stetter. The reaction product is a 1,4 dicarbonyl compound. The active catalyst can be a… …   Wikipedia

  • Conrad Willgerodt — Born November 2, 1841(1841 11 02) Harlingerode, Duchy of Brunswick, today Bad Harzburg, Germany Died December 19 …   Wikipedia

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